Strategic Prevention
Framework for Prescription Drugs (SPF-Rx)
Revision of a currently approved collection
No
Regular
05/13/2020
Requested
Previously Approved
36 Months From Approved
01/31/2021
321
204
1,869
618
0
0
The SPF-Rx program is designed to
address nonmedical use of prescription drugs as well as opioid
overdoses by raising awareness about the dangers of sharing
medications and by working with pharmaceutical and medical
communities. The SPF-Rx program aims to promote collaboration
between states/tribes and pharmaceutical and medical communities to
understand the risks of overprescribing to youth age 12–17 and
adults 18 years of age and older and enhance capacity for and
access to Prescription Drug Monitoring Program (PDMP) data for
prevention purposes.
US Code:
42
USC 516 Name of Law: Healthy Pople 2020 Substance Abuse Yopic
Area HP 2020-SA
Currently, there are 618 total
burden hours. SAMHSA is requesting 1,867.5 burden hours. This is an
adjustment of 1,249.5 hours based on actual burden estimates
revisions to data collection instruments. This equates to an
overall increase of 1,249.5 hours and $15,504.06 over the
previously approved data collection.The annual burden costs have
increased from previous approval due to 4 factors: 1. The previous
OMB approval estimated 100 AII responses (25 grantees and 75
subrecipients), but the SPF-Rx grantees currently have 25 grantees
and 123 subrecipients, totaling 148 AII responses, accounting for
an additional 48 responses, 192 hours and $4,974.72 per year of
data collection with the entire grantee cohort (i.e., Years 4 and
5). 2. The previous OMB approval estimated only 25 Community-Level
Outcomes Module responses, but one is completed for each
subrecipient, and therefore the burden has been increased to 123
responses, accounting for an additional 98 responses, 343 hours,
and $14,961.66 per year of data collection with the entire grantee
cohort (i.e., Years 4 and 5). 3. Based on grantee feedback, the
time it takes for respondents to complete the AII was increased
from 2.3 hours to 4 hours. While grantee feedback indicated that
the Grantee-Level Outcomes Module burden should be increased from 3
hours to 6.2 hours, the module was reduced and the burden decreased
to 2.5 hours. The Community-Level Outcomes Module burden was
initially increased from 3 hours to 3.5 hours based on grantee
feedback, but the instrument was subsequently reduced and the
burden now estimated at 1.25 hours. The adjustments in the three
instruments results in an overall reduction of 55 hours and
$2,248.4 per year of data collection with the entire grantee cohort
(i.e., Years 4 and 5). This reflects a 42% decrease in burden for
the Grantee-Level Outcomes and the Community-Level Outcomes Modules
(decrease from 6 hours to 3.75 hours across all respondents in all
years). We expect that these burden estimates are more accurate
than previous burden estimates, given that they are based on
feedback from those who have completed data collection efforts
during Years 1 and 2 of the evaluation in addition to changes in
the data collection instruments based on the identification of
duplicative data elements. 4. The SPF-Rx hourly wage estimates in
the previous statement were $40.88, based on one salary using 2015
Bureau of Labor Statistics (BLS) data. The current package
increased grantee-level staff to 2018 BLS data for hourly wages of
$43.62. BLS data are an accurate representation of salary data,
utilizing the National Compensation Survey which provides
comprehensive measures of compensation cost trends and is updated
each year to reflect those changes in average compensation.
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.